Canonical Allele Identifier: CA216859242

Gene: CYP2E1

Linked Data

• dbSNP Id: rs557594682
• gnomAD v2: 10-135352686-T-A
• gnomAD v3: 10-133539182-T-A
• gnomAD v4: 10-133539182-T-A
• MyVariant Identifiers: chr10:g.135352686T>A (hg19) ; chr10:g.133539182T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133539182T>A , CM000672.2:g.133539182T>A	GRCh38
NC_000010.10:g.135352686T>A , CM000672.1:g.135352686T>A	GRCh37
NC_000010.9:g.135202676T>A	NCBI36
NG_008383.1:g.16820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368520.1:n.1358+1290T>A